Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

1201 to 1203 of 1203 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1201	9963	SLC23A1	Solute carrier family 23 member 1	SLC23A2, SVCT1, YSPL3	Cholestasis, Respiratory failure
1202	9990	SLC12A6	Solute carrier family 12 member 6	ACCPN, CMT2II, KCC3, KCC3A, KCC3B	Acrocephaly, Agenesis of corpus callosum, Aqueductal stenosis, Barrett esophagus, Bipolar disorder, Brachycephaly, Camptodactyly of fingers, Corpus callosum agenesis neuronopathy, Corpus callosum agenesis-neuronopathy syndrome, Craniosynostosis, Developmental delay, Hemiplegia/hemiparesis, High palate, Hypoplasia of the maxilla, Macrotia View all (15 more)
1203	9997	SCO2	Synthesis of cytochrome C oxidase 2	CEMCOX1, ECGF1, Gliostatin, MC4DN2, MYP6, PD-ECGF, SCO1L, TP, TYMP, TdRPase	Anemia, Cardioencephalomyopathy, Cardiomyopathy, Central nervous system inborn metabolic diseases, Charcot-marie-tooth disease, Congestive heart failure, Cytochrome-c oxidase deficiency, Developmental delay, Developmental regression, Dysarthria, Dyskinetic syndrome, Dysphagia, Exotropia, Fatal cytochrome c oxidase deficiency, Hypertrichosis View all (24 more)

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